NIR-Laser-Controlled Drug Release from DOX/IR-780-Loaded Temperature-Sensitive-Liposomes for Chemo-Photothermal Synergistic Tumor Therapy

被引:141
|
作者
Yan, Fei [1 ]
Duan, Wanlu [2 ]
Li, Yekuo [2 ]
Wu, Hao [3 ]
Zhou, Yuli [4 ,5 ]
Pan, Min [1 ]
Liu, Hongmei [3 ]
Liu, Xin [1 ]
Zheng, Hairong [1 ,3 ,6 ]
机构
[1] Chinese Acad Sci, Shenzhen Inst Adv Technol, Inst Biomed & Hlth Engn, Paul C Lauterbur Res Ctr Biomed Imaging, Shenzhen, Peoples R China
[2] Guangzhou Gen Hosp Guangzhou Mil Command, Dept Ultrasound, Guangzhou, Guangdong, Peoples R China
[3] Southern Med Univ, Affiliated Hosp 3, Dept Ultrasonog, Acad Orthoped Guangdong Prov, Guangzhou, Guangdong, Peoples R China
[4] Jinan Univ, Shenzhen Peoples Hosp, Dept Ultrasonog, Shenzhen, Peoples R China
[5] Jinan Univ, Clin Med Coll 2, Shenzhen, Peoples R China
[6] Chinese Acad Sci, Shenzhen Inst Adv Technol, Shenzhen Key Lab Nanobiomech, Shenzhen, Peoples R China
来源
THERANOSTICS | 2016年 / 6卷 / 13期
基金
中国国家自然科学基金;
关键词
Photothermal therapy; Temperature-sensitive-liposome; IR-780; Doxorubicin; Breast tumors; SERUM-ALBUMIN NANOPARTICLES; IN-VIVO; CANCER-CELLS; THERMOSENSITIVE LIPOSOMES; PHOTODYNAMIC THERAPY; BREAST-CANCER; COMBINATION THERAPY; MILD HYPERTHERMIA; DELIVERY; DOXORUBICIN;
D O I
10.7150/thno.14937
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
NIR laser-induced photothermal therapy (PTT) through near-infrared agents has demonstrated the great potential in solid tumor ablation. However, the nonuniform heat distribution over tumors from PTT makes it insufficient to kill all tumor cells, resulting in tumor recurrence and inferior outcomes. To improve the tumor treatment efficacy, it is highly desirable to develop the combinational treatment of PTT with other modalities, especially with chemotherapeutic agents. Here we report a smart DOX/IR-780-loaded temperature-sensitive-liposome (DITSL) which can achieve NIR-laser-controlled drug release for chemo-photothermal synergistic tumor therapy. In this system, the liposoluble IR-780 was incorporated into the temperature-sensitive lipid bilayer and the soluble chemotherapeutic doxorubicin (DOX) was encapsulated in the hydrophilic core. The resulting DITSL is proved to be physiologically stable and can provide a fast and laser irradiation-controllable DOX release in the PBS and cellular conditions. We further employed this nanoparticle for tumor treatment, demonstrating significantly higher tumor inhibition efficacy than that of DOX-loaded temperature-sensitive-liposome (DTSL) or IR780-loaded temperature-sensitive-liposome (ITSL) in the in vitro cells and in vivo animals. Histological analysis further revealed much more apoptotic cells, confirming the advantageous anti-tumor effect of DITSL over DTSL or ITSL. Our study provides a promising strategy to realize chemo-photothermal synergistic combination therapy for breast tumors.
引用
收藏
页码:2337 / 2351
页数:15
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